Proof-of-concept rare cancers in drug development: The case for rhabdomyosarcoma

E. Sokolowski, C. B. Turina, K. Kikuchi, D. M. Langenau, C. Keller

Research output: Contribution to journalReview article

19 Scopus citations

Abstract

Rare diseases typically affect fewer than 200 000 patients annually, yet because thousands of rare diseases exist, the cumulative impact is millions of patients worldwide. Every form of childhood cancer qualifies as a rare disease - including the childhood muscle cancer, rhabdomyosarcoma (RMS). The next few years promise to be an exceptionally good era of opportunity for public-private collaboration for rare and childhood cancers. Not only do certain governmental regulation advantages exist, but these advantages are being made permanent with special incentives for pediatric orphan drug-product development. Coupled with a growing understanding of sarcoma tumor biology, synergy with pharmaceutical muscle disease drug-development programs, and emerging publically available preclinical and clinical tools, the outlook for academic-community-industry partnerships in RMS drug development looks promising.

Original languageEnglish (US)
Pages (from-to)1877-1889
Number of pages13
JournalOncogene
Volume33
Issue number15
DOIs
StatePublished - Apr 10 2014

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Keywords

  • biomarker
  • drug development
  • kinase
  • proof-of-concept disease
  • rare cancers
  • rhabdomyosarcoma

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Cite this

Sokolowski, E., Turina, C. B., Kikuchi, K., Langenau, D. M., & Keller, C. (2014). Proof-of-concept rare cancers in drug development: The case for rhabdomyosarcoma. Oncogene, 33(15), 1877-1889. https://doi.org/10.1038/onc.2013.129